Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs41341748
rs41341748
0.060 GeneticVariation BEFREE We examined polymorphisms within ELAC2 (S217L, A541T, E622V), MSR1 (P275A, R293X, aIVS5-59c), and RNASEL (E265X, R462Q, D541E) in 150 European-Americans with metastatic prostate cancer and 170 prostate cancer-free controls using pyrosequencing assays. 16114055

2006

dbSNP: rs41341748
rs41341748
0.060 GeneticVariation BEFREE Of note, carriers of R293X were equally frequent in 367 sporadic prostate cancer cases (1.9%) and in 197 controls (2.0%). 16287155

2006

dbSNP: rs41341748
rs41341748
0.060 GeneticVariation BEFREE Several variants were significantly or marginally significantly associated with sporadic, not hereditary PCa risk, including R293X in white men (random effect OR = 1.34, P = 0.09) and D174Y in black men (random effect OR = 2.41, P = 0.04). 16425212

2006

dbSNP: rs41341748
rs41341748
0.060 GeneticVariation BEFREE Meta-analyses revealed significant associations of prostate cancer with MSR1 IVS7delTTA, -14,742 A>G, and Arg293X in European Americans; Asp174Tyr in African Americans; RNASEL Arg462Gln in European American's overall and in family history-negative disease; and Glu265X in family history-positive European Americans. 15824169

2005

dbSNP: rs41341748
rs41341748
0.060 GeneticVariation BEFREE Macrophage scavenger receptor 1 999C>T (R293X) mutation and risk of prostate cancer. 15734964

2005

dbSNP: rs41341748
rs41341748
0.060 GeneticVariation BEFREE Our results suggest that mutations in MSR1 gene might play a role in prostate cancer susceptibility, particularly the R293X mutation. 15042613

2004

dbSNP: rs2229388
rs2229388
0.030 GeneticVariation BEFREE Based on our meta-analysis, the P275A polymorphism in the MSR1 gene is unlikely to be a risk factor for PCa. 26225686

2015

dbSNP: rs2229388
rs2229388
0.030 GeneticVariation BEFREE The haplotype frequencies were significantly different between localized prostate cancer cases and controls, with a global P value of 0.004, and the haplotype containing the minor alleles of the P275A and INDEL7 variants was associated with a significantly reduced risk of localized prostate cancer (odds ratio = 0.28, 95% CI 0.13-0.59), relative to the most common haplotype. 17768178

2007

dbSNP: rs2229388
rs2229388
0.030 GeneticVariation BEFREE Of the eight variants that affect the encoded protein (splice site, nonsense, and missense), only R293X as well as the polymorphism c.823C>G (P275A) were additionally present at remarkable frequencies in further samples of sporadic prostate cancer and controls. 16287155

2006

dbSNP: rs72552387
rs72552387
0.030 GeneticVariation BEFREE Several variants were significantly or marginally significantly associated with sporadic, not hereditary PCa risk, including R293X in white men (random effect OR = 1.34, P = 0.09) and D174Y in black men (random effect OR = 2.41, P = 0.04). 16425212

2006

dbSNP: rs72552387
rs72552387
0.030 GeneticVariation BEFREE Meta-analyses revealed significant associations of prostate cancer with MSR1 IVS7delTTA, -14,742 A>G, and Arg293X in European Americans; Asp174Tyr in African Americans; RNASEL Arg462Gln in European American's overall and in family history-negative disease; and Glu265X in family history-positive European Americans. 15824169

2005

dbSNP: rs72552387
rs72552387
0.030 GeneticVariation BEFREE In our sample, the rare Asp174Tyr missense change was identified nearly twice as frequently in men with prostate cancer (6.8%) compared with unaffected controls (3.6%; P = 0.14). 12839931

2003

dbSNP: rs3747531
rs3747531
0.010 GeneticVariation BEFREE Minor alleles of rs2243250 (T) in IL4 (OR = 1.46, 95% CI 1.03-2.08, P-trend = 0.03), rs1800896 (G) in IL10 (OR = 0.77, 95% CI 0.61-0.96, P-trend = 0.02), rs2430561 (A) in IFNG (OR = 1.33, 95% CI 1.02-1.74; P-trend = 0.04), rs3747531 (C) in MSR1 (OR = 0.55, 95% CI 0.32-0.95; P-trend = 0.03), and possibly rs4073 (A) in IL8 (OR = 0.81, 95% CI 0.64-1.01, P-trend = 0.06) were associated with higher- (Gleason 7-10; N = 222), but not lower- (Gleason 2-6; N = 380) grade prostate cancer. 28317149

2017

dbSNP: rs2127565
rs2127565
0.010 GeneticVariation BEFREE Our study provides the proof-of-principle that some of the genetic variants (such as rs486907, rs627928 and rs2127565) in genes RNASEL, MSR1 and ELAC2 can be used as predictors of aggressiveness and progression of PCa. 26251261

2015

dbSNP: rs369108477
rs369108477
0.010 GeneticVariation BEFREE Our large-scale analysis of case and controls from several countries found no evidence that the 999C>T mutation is associated with increased risk of prostate cancer. 15734964

2005